Logan Walker
6PUBLICATIONS
109CO-AUTHORS
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Publications (6)
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|Oct 06, 2022
Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers.Christopher Hakkaart, John F Pearson, Louise Marquart
|Aug 18, 2022
Clinical, splicing, and functional analysis to classify BRCA2 exon 3 variants: Application of a points-based ACMG/AMP approach.Mads Thomassen, Romy L S Mesman, Thomas V O Hansen
|Jan 19, 2022
Rare germline copy number variants (CNVs) and breast cancer risk.Joe Dennis, Jonathan P Tyrer, Logan C Walker
|Jul 21, 2021
Increased gene expression variability in BRCA1-associated and basal-like breast tumours.George A R Wiggins, Michael A Black, Anita Dunbier
|Oct 06, 2020
Detecting rare copy number variants from Illumina genotyping arrays with the CamCNV pipeline: Segmentation of z-scores improves detection and reliability.Joe Dennis, Logan Walker, Jonathan Tyrer
|Jan 10, 2019
Targeted RNA-seq successfully identifies normal and pathogenic splicing events in breast/ovarian cancer susceptibility and Lynch syndrome genes.Rita D Brandão, Klaas Mensaert, Irene López-Perolio
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Frequent Collaborators
3 joint publications
Ana Vega
3 joint publications
Miguel de la Hoya
3 joint publications
Amanda B Spurdle
3 joint publications
Joe Dennis
2 joint publications
Heli Nevanlinna
2 joint publications
Anna Jakubowska
2 joint publications
Paolo Peterlongo
2 joint publications
Irene L Andrulis
2 joint publications
Kyriaki Michailidou
2 joint publications
Marinus J Blok
